At a Glance
- Tasks: Join us as a Principal Statistical Programmer, supporting diverse projects and leading teams.
- Company: Veramed is a unique CRO focused on quality consultancy and employee growth.
- Benefits: Enjoy remote or hybrid work options, competitive pay, and extensive training support.
- Other info: Gain leadership experience while managing key client projects and mentoring staff.
- Why this job: Be part of a friendly environment that values personal and professional development.
- Qualifications: BSc, MSc or PhD in a numerical discipline with 6+ years of industry experience required.
The predicted salary is between 36000 - 60000 £ per year.
Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth.
We have an exciting opportunity for a Principal level Statistical Programmer to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive package.
The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).
Key ResponsibilitiesThe job tasks listed below outline the scope of the position. The application of these tasks may vary based on current business needs.
Technical- Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
- Author, review and approve study TFL shells and dataset specifications
- Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice
- Identify data issues and outliers
- Complete, review and approve CDISC Validation tool reports
- Identify data and standards issues and resolve or escalate as appropriate
- Awareness of emerging standards and associated impact to ongoing and future planned trials
- Maintain proficiency in SAS and awareness of developments
- Maintain study master file documents and any other documents that are required to be audit ready
- Line management of statisticians, programmers and other technical staff. Accountable for overall performance of direct reports
- Provide coaching and mentoring of staff to achieve “excellence”. Direct employee career development and ensure line reports receive appropriate training to perform their day-to-day jobs
- Interview and effectively on-board and integrate new staff members
- Provide programming technical leadership and coaching
- Oversight of key client projects/portfolios. To include:
- Being Veramed Project Manager on client accounts and projects
- Maintain the project plan
- Proactive management of resource, scope change and risks
- Manage the delivery of projects to budget
- Manage client expectations and issue resolution
- Lead internal and client study, project and cross functional team meetings effectively
- Present study updates internally and at client meetings
- Share scientific, technical and practical knowledge within the team and with colleagues
- Perform work in full compliance with applicable internal and client policies, procedures, processes and training
- Build effective collaborative working relationships with internal and client team members
- Ensure learnings are shared across projects or studies
- Develop and provide internal technical training where appropriate
- Lead process improvement initiatives
- BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
- At least 6 years of relevant industry experience
- Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
A warm, friendly working environment in which to thrive both personally and professionally. A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level. A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry. The ability to own your role and develop your skills and experience.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Statistical Programmer - Remote, Office or Hybrid - UK in London
✨Tip Number 1
Familiarise yourself with the latest trends and standards in statistical programming, particularly in SAS. This will not only enhance your technical skills but also demonstrate your commitment to staying current in the field during interviews.
✨Tip Number 2
Network with professionals in the clinical trial and statistical programming community. Attend relevant webinars or conferences to connect with potential colleagues and learn more about Veramed's culture and projects.
✨Tip Number 3
Prepare to discuss your experience in managing projects and teams. Highlight specific examples where you successfully led a project or mentored junior staff, as this aligns with the supervisory aspects of the role.
✨Tip Number 4
Research Veramed’s approach to employee development and their unique working environment. Be ready to articulate how you can contribute to and benefit from their supportive culture during your discussions.
We think you need these skills to ace Principal Statistical Programmer - Remote, Office or Hybrid - UK in London
Some tips for your application 🫡
Understand the Role:Before applying, make sure you fully understand the responsibilities and requirements of the Principal Statistical Programmer position. Familiarise yourself with the key tasks mentioned in the job description, such as programming support, project management, and people management.
Tailor Your CV:Customise your CV to highlight relevant experience and skills that align with the job description. Emphasise your proficiency in SAS, your experience in clinical trial processes, and any leadership roles you've held. Use specific examples to demonstrate your achievements.
Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for the role and the company. Mention why you are interested in Veramed and how your background makes you a suitable candidate. Be sure to address your understanding of the clinical drug development process and your commitment to excellence.
Proofread Your Application:Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a role that involves data accuracy and compliance.
How to prepare for a job interview at Veramed
✨Showcase Your Technical Expertise
As a Principal Statistical Programmer, you'll need to demonstrate your proficiency in SAS and your understanding of clinical trial documents. Be prepared to discuss specific projects where you've authored or validated SAS programs, and highlight any experience with CDISC standards.
✨Emphasise People Management Skills
Since the role involves line management and mentoring, share examples of how you've successfully led teams in the past. Discuss your approach to coaching and developing staff, as well as any experience you have in managing client expectations and project delivery.
✨Prepare for Project Management Questions
Expect questions about your project management experience, especially regarding resource management and risk assessment. Be ready to provide examples of how you've maintained project plans and delivered projects within budget while managing client relationships.
✨Demonstrate Your Collaborative Spirit
Veramed values collaboration, so be sure to highlight your ability to build effective working relationships. Share instances where you've worked cross-functionally or led team meetings, and discuss how you ensure knowledge sharing and process improvements within your team.
